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Pediatric Collagenous Gastroenterocolitis Successfully Treated with Methotrexate.
Beate C Beinvogl1, Jeffrey D Goldsmith2, Ramalingam Arumugam3
1Division of Gastroenterology, Boston Children's Hospital, Boston, MA, USA.
A pediatric patient with collagenous gastroenterocolitis experienced symptom recurrence after medication withdrawal. Treatment with immunosuppressants and corticosteroids led to sustained remission, highlighting therapeutic options for this rare condition.
Area of Science:
- Gastroenterology
- Pediatric Gastroenterology
- Immunology
Background:
- Collagenous gastroenterocolitis is a rare inflammatory bowel disease characterized by a collagen layer deposition in the colon.
- It often presents with chronic watery diarrhea, malabsorption, and failure to thrive, particularly in pediatric populations.
Observation:
- A previously healthy two-and-a-half-year-old female presented with prolonged watery diarrhea, emesis, and fevers, leading to severe hypoalbuminemia and hypogammaglobulinemia.
- Endoscopic and colonoscopic biopsies confirmed collagenous gastroenterocolitis, necessitating parenteral nutrition due to persistent symptoms.
Findings:
- The patient initially responded to prednisone but relapsed upon transitioning to budesonide.
- Intravenous prednisone followed by intramuscular methotrexate induced a 15-month remission.
- Recurrence of collagenous colitis after methotrexate cessation responded well to a short course of oral budesonide, achieving sustained remission.
Implications:
- This case highlights the potential efficacy of combined immunosuppressive and corticosteroid therapy in managing refractory pediatric collagenous gastroenterocolitis.
- The findings suggest a potential role for methotrexate in long-term maintenance therapy for this condition.
- Successful budesonide retreatment indicates its utility in managing relapses, even after prior treatment failures.
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